Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000288.3 | 520 | Missense Mutation | TCC,TTC | S25F | NP_000279.1 |
XM_005267019.4 | 520 | Intron | XP_005267076.1 | ||
XM_006715502.1 | 520 | Missense Mutation | TCC,TTC | S25F | XP_006715565.1 |
XM_017010934.1 | 520 | Missense Mutation | TCC,TTC | S25F | XP_016866423.1 |